Variant report

Variant	nsv527464
Chromosome Location	chr1:246698653-246742157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1153)
CpG islands
(count:1100)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246729530-246729980	K562	blood:	n/a	n/a
2	ARID3A	chr1:246732646-246733496	K562	blood:	n/a	n/a
3	ARID3A	chr1:246730285-246730981	K562	blood:	n/a	n/a
4	ARID3A	chr1:246739546-246739738	K562	blood:	n/a	n/a
5	ARID3A	chr1:246740073-246740316	K562	blood:	n/a	n/a
6	ARID3A	chr1:246729459-246729909	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:246729043-246729235	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:246740858-246741585	K562	blood:	n/a	chr1:246741392-246741408 chr1:246741393-246741409
9	ATF1	chr1:246730636-246730930	K562	blood:	n/a	n/a
10	ATF1	chr1:246740996-246741399	K562	blood:	n/a	n/a
11	ATF1	chr1:246740536-246740756	K562	blood:	n/a	n/a
12	ATF1	chr1:246732872-246733329	K562	blood:	n/a	n/a
13	ATF2	chr1:246729326-246729950	GM12878	blood:	n/a	n/a
14	ATF2	chr1:246729219-246729717	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:246729048-246729793	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr1:246729298-246730096	GM12878	blood:	n/a	n/a
17	ATF3	chr1:246729163-246730103	A549	lung:	n/a	n/a
18	ATF3	chr1:246729333-246729841	A549	lung:	n/a	n/a
19	ATF3	chr1:246734658-246735052	K562	blood:	n/a	n/a
20	BACH1	chr1:246729303-246730285	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr1:246732997-246733252	K562	blood:	n/a	n/a
22	BACH1	chr1:246741033-246741336	K562	blood:	n/a	n/a
23	BACH1	chr1:246730812-246730950	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:246729185-246729841	K562	blood:	n/a	n/a
25	BACH1	chr1:246730246-246730860	K562	blood:	n/a	n/a
26	BCL3	chr1:246728974-246730135	A549	lung:	n/a	chr1:246729609-246729618
27	BCL3	chr1:246729188-246730094	A549	lung:	n/a	chr1:246729609-246729618
28	BCLAF1	chr1:246729186-246730406	K562	blood:	n/a	chr1:246730329-246730338 chr1:246729609-246729618
29	BCLAF1	chr1:246729322-246730368	GM12878	blood:	n/a	chr1:246730329-246730338 chr1:246729609-246729618
30	BCLAF1	chr1:246740984-246741507	K562	blood:	n/a	n/a
31	BCLAF1	chr1:246729321-246730493	GM12878	blood:	n/a	chr1:246730329-246730338 chr1:246729609-246729618
32	BHLHE40	chr1:246740142-246740277	K562	blood:	n/a	n/a
33	BHLHE40	chr1:246741097-246741846	K562	blood:	n/a	n/a
34	BHLHE40	chr1:246734762-246735089	K562	blood:	n/a	n/a
35	BHLHE40	chr1:246732671-246732792	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:246732995-246733247	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:246736925-246737078	A549	lung:	n/a	n/a
38	BHLHE40	chr1:246739423-246739805	K562	blood:	n/a	chr1:246739593-246739614 chr1:246739599-246739608 chr1:246739597-246739610 chr1:246739599-246739608 chr1:246739600-246739609
39	BHLHE40	chr1:246729128-246730340	K562	blood:	n/a	n/a
40	BHLHE40	chr1:246729205-246730577	GM12878	blood:	n/a	n/a
41	BRCA1	chr1:246729656-246729924	GM12878	blood:	n/a	n/a
42	BRCA1	chr1:246729270-246730083	HepG2	liver:	n/a	n/a
43	BRCA1	chr1:246729148-246731037	Hela-S3	cervix:	n/a	chr1:246730282-246730289
44	BRCA1	chr1:246729362-246729742	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr1:246729309-246729908	K562	blood:	n/a	n/a
46	CBX3	chr1:246724108-246724521	K562	blood:	n/a	n/a
47	CBX3	chr1:246728688-246730512	K562	blood:	n/a	n/a
48	CCNT2	chr1:246729289-246730481	K562	blood:	n/a	n/a
49	CCNT2	chr1:246740958-246741313	K562	blood:	n/a	n/a
50	CEBPB	chr1:246721402-246721657	K562	blood:	n/a	chr1:246721504-246721515

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246729572-246729622	AG04449	skin:	fetal
2	chr1:246729501-246729551	NB4	blood:	n/a
3	chr1:246729572-246729622	AG04449	skin:	fetal
4	chr1:246729501-246729551	NB4	blood:	n/a
5	chr1:246729459-246729509	T-47D	breast:	n/a
6	chr1:246729218-246729268	SK-N-MC	brain:	n/a
7	chr1:246730188-246730238	HIPEpiC	eye:	n/a
8	chr1:246730185-246730235	GM19239	blood:	n/a
9	chr1:246730185-246730235	RPTEC	kidney:	n/a
10	chr1:246729345-246729395	AG04450	lung:	fetal
11	chr1:246729875-246729925	Hepatocyte	liver:	n/a
12	chr1:246733057-246733107	HRCEpiC	kidney:	n/a
13	chr1:246729501-246729551	AG04449	skin:	fetal
14	chr1:246730219-246730269	Jurkat	blood:	n/a
15	chr1:246729218-246729268	T-47D	breast:	n/a
16	chr1:246729875-246729925	NB4	blood:	n/a
17	chr1:246729345-246729395	Caco-2	colon:	n/a
18	chr1:246729501-246729551	AG09309	skin:	n/a
19	chr1:246730185-246730235	HEK293	kidney:	embryo
20	chr1:246729578-246729628	ProgFib	skin:	n/a
21	chr1:246730185-246730235	HNPCEpiC	eye:	n/a
22	chr1:246728677-246728727	HCT-116	colon:	n/a
23	chr1:246728677-246728727	CMK	blood:	n/a
24	chr1:246729218-246729268	GM19239	blood:	n/a
25	chr1:246729345-246729395	HIPEpiC	eye:	n/a
26	chr1:246729572-246729622	MCF10A-Er-Src	breast:	n/a
27	chr1:246729218-246729268	AG09319	gingival:	n/a
28	chr1:246729875-246729925	SAEC	small airway:	n/a
29	chr1:246729578-246729628	NHBE	bronchial:	n/a
30	chr1:246729578-246729628	NB4	blood:	n/a
31	chr1:246728727-246728777	HRPEpiC	eye:	n/a
32	chr1:246728677-246728727	H1-hESC	embryonic stem cell:	embryo
33	chr1:246729572-246729622	SAEC	small airway:	n/a
34	chr1:246729875-246729925	A549	lung:	n/a
35	chr1:246729669-246729719	CMK	blood:	n/a
36	chr1:246729669-246729719	K562	blood:	n/a
37	chr1:246729585-246729635	Caco-2	colon:	n/a
38	chr1:246729875-246729925	AG09309	skin:	n/a
39	chr1:246728677-246728727	AoSMC	blood vessel:	n/a
40	chr1:246730185-246730235	HRE	kidney:	n/a
41	chr1:246729578-246729628	GM12878	blood:	n/a
42	chr1:246729875-246729925	HIPEpiC	eye:	n/a
43	chr1:246729875-246729925	SK-N-MC	brain:	n/a
44	chr1:246717609-246717659	A549	lung:	n/a
45	chr1:246729578-246729628	AG04450	lung:	fetal
46	chr1:246728727-246728777	HNPCEpiC	eye:	n/a
47	chr1:246741712-246741762	AG10803	skin:	n/a
48	chr1:246730185-246730235	HMEC	breast:	n/a
49	chr1:246729345-246729395	Hela-S3	cervix:	n/a
50	chr1:246729345-246729395	NHDF-neo	bronchial:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246729068..246729614-chr3:149530492..149531281,2	Hela-S3	cervix:
2	chr1:246738601..246740180-chr1:246754340..246756772,2	MCF-7	breast:
3	chr1:246711201..246713601-chr1:246713604..246715628,2	K562	blood:
4	chr1:246692831..246695438-chr1:246704915..246707883,3	K562	blood:
5	chr1:246729197..246730166-chr14:75745608..75746363,2	Hela-S3	cervix:
6	chr1:246715254..246718890-chr1:246721529..246724491,4	K562	blood:
7	chr1:246668302..246670787-chr1:246727323..246729930,4	MCF-7	breast:
8	chr1:246698102..246699613-chr1:246703690..246706174,2	K562	blood:
9	chr1:246724443..246726246-chr1:246728599..246730567,2	MCF-7	breast:
10	chr1:246699626..246702195-chr1:246706012..246708369,2	MCF-7	breast:
11	chr1:246699626..246702195-chr1:246706012..246708369,2	MCF-7	breast:
12	chr1:246715254..246718890-chr1:246721529..246724491,4	K562	blood:
13	chr1:246704378..246705938-chr1:246830141..246833108,2	K562	blood:
14	chr1:246711666..246713604-chr1:246728356..246731058,3	K562	blood:
15	chr1:246698102..246699613-chr1:246703690..246706174,2	K562	blood:
16	chr1:246715254..246717905-chr1:246720739..246723913,4	K562	blood:
17	chr1:246697803..246699754-chr1:246703795..246706062,2	K562	blood:
18	chr1:246703270..246704853-chr1:247491463..247493395,2	K562	blood:
19	chr1:246693616..246696084-chr1:246696950..246700656,3	K562	blood:
20	chr1:246730131..246732589-chr1:246747162..246749763,2	MCF-7	breast:
21	chr1:246729017..246731987-chr1:246738180..246742192,5	MCF-7	breast:
22	chr1:246711201..246713601-chr1:246713604..246715628,2	K562	blood:
23	chr1:246694155..246697194-chr1:246698575..246701434,3	MCF-7	breast:
24	chr1:226185428..226188059-chr1:246740463..246742577,2	K562	blood:
25	chr1:246728909..246731573-chr1:246733348..246738076,5	MCF-7	breast:
26	chr1:19638692..19639192-chr1:246729163..246730124,2	Hela-S3	cervix:
27	chr1:246715254..246717905-chr1:246720739..246723913,4	K562	blood:
28	chr1:246685591..246688881-chr1:246727054..246730014,3	K562	blood:
29	chr1:246729874..246731842-chr1:246862649..246864902,2	K562	blood:
30	chr1:246729967..246732161-chr22:19156837..19159425,2	K562	blood:
31	chr1:246739822..246741667-chr1:246766063..246767788,2	K562	blood:
32	chr1:246660669..246662784-chr1:246700415..246702206,2	MCF-7	breast:
33	chr1:246697803..246699754-chr1:246703795..246706062,2	K562	blood:
34	chr1:246722538..246724149-chr1:246820776..246822354,2	K562	blood:
35	chr1:246727699..246730587-chr1:246733873..246736383,3	MCF-7	breast:
36	chr1:246668048..246670638-chr1:246738189..246740927,2	K562	blood:
37	chr1:246719266..246723453-chr1:246727295..246731122,5	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMYD3-4	chr1:246715093-246715408	NONHSAT010710
2	lnc-SMYD3-4	chr1:246714169-246714819	NONHSAT010710

No data

Variant related genes	Relation type
CNST	TF binding region
TFB2M	TF binding region
CNST	CpG island
TFB2M	CpG island
ENSG00000162852	chromatin interactions
ENSG00000242042	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000162714	chromatin interactions
ENSG00000040487	chromatin interactions
ENSG00000162851	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000143751	chromatin interactions
ENSG00000227728	chromatin interactions
ENSG00000260924	chromatin interactions

Extended variants
information (count: 2245 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2245 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3120693	chr1:246698653-246698654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191695111	chr1:246698681-246698682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547638578	chr1:246698690-246698691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565730814	chr1:246698760-246698761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138205340	chr1:246698823-246698824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372211610	chr1:246698828-246698829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201673598	chr1:246698835-246698836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375035216	chr1:246698836-246698837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74163459	chr1:246698839-246698840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147009391	chr1:246698840-246698841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35055001	chr1:246698842-246698843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35054446	chr1:246698888-246698889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs61842566	chr1:246698898-246698899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs56693991	chr1:246698918-246698919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11523794	chr1:246698936-246698937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs371630378	chr1:246698945-246698946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562544170	chr1:246698965-246698966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11523791	chr1:246698970-246698971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183754904	chr1:246698973-246698974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11523792	chr1:246698981-246698982	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs192931189	chr1:246699015-246699016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546663936	chr1:246699018-246699019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2879858	chr1:246699030-246699031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532336089	chr1:246699049-246699050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554386794	chr1:246699074-246699075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569282042	chr1:246699117-246699118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537728231	chr1:246699118-246699119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548499425	chr1:246699122-246699123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568228691	chr1:246699126-246699127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533979403	chr1:246699149-246699150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77885668	chr1:246699161-246699162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534672211	chr1:246699214-246699215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71638360	chr1:246699237-246699238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80071185	chr1:246699254-246699255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539978532	chr1:246699255-246699256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61168782	chr1:246699295-246699296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61511024	chr1:246699307-246699308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555861754	chr1:246699308-246699309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576019210	chr1:246699361-246699362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2340786	chr1:246699376-246699377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs561645809	chr1:246699377-246699378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2340787	chr1:246699387-246699388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs543480681	chr1:246699394-246699395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12755629	chr1:246699403-246699404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs574028687	chr1:246699411-246699412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560357642	chr1:246699458-246699459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182100342	chr1:246699480-246699481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142200473	chr1:246699492-246699493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562724044	chr1:246699530-246699531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559557225	chr1:246699575-246699576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	19805367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	CNVD

Chromatin state (count:1883 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246691200-246703000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr1:246691400-246702000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:246694400-246704000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr1:246694400-246704200	Weak transcription	Left Ventricle	heart
5	chr1:246694600-246706600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:246694800-246706600	Weak transcription	Right Ventricle	heart
7	chr1:246697400-246704200	Weak transcription	Lung	lung
8	chr1:246698000-246705000	Weak transcription	Small Intestine	intestine
9	chr1:246698200-246700400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:246698200-246703600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:246698200-246705800	Weak transcription	NHLF	lung
12	chr1:246698800-246703000	Weak transcription	Ovary	ovary
13	chr1:246699000-246702200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:246699200-246701400	Weak transcription	Primary B cells from cord blood	blood
15	chr1:246699200-246702200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:246699200-246705800	Weak transcription	HUVEC	blood vessel
17	chr1:246699400-246701800	Weak transcription	Liver	Liver
18	chr1:246699400-246702000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:246699400-246706200	Weak transcription	Spleen	Spleen
20	chr1:246699600-246701600	Weak transcription	Fetal Muscle Leg	muscle
21	chr1:246699600-246702000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:246699600-246702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:246699600-246703200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:246699600-246704200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:246699600-246704200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr1:246699800-246702000	Weak transcription	Primary T cells from cord blood	blood
27	chr1:246699800-246702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:246699800-246703200	Weak transcription	Primary B cells from peripheral blood	blood
29	chr1:246699800-246703800	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr1:246699800-246704000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:246699800-246704200	Weak transcription	GM12878-XiMat	blood
32	chr1:246699800-246704600	Weak transcription	Aorta	Aorta
33	chr1:246699800-246705200	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr1:246699800-246705200	Weak transcription	NHDF-Ad	bronchial
35	chr1:246700000-246702000	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr1:246700000-246702000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:246700000-246702800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr1:246700000-246704200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:246700000-246705600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:246700200-246702000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:246700200-246702000	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr1:246700200-246702200	Weak transcription	Adipose Nuclei	Adipose
43	chr1:246700200-246702200	Weak transcription	Fetal Intestine Small	intestine
44	chr1:246700200-246702200	Weak transcription	Fetal Stomach	stomach
45	chr1:246700200-246702400	Weak transcription	Brain Hippocampus Middle	brain
46	chr1:246700200-246703000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr1:246700200-246703800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr1:246700200-246706400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr1:246700400-246701800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:246700400-246702200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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